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EPR Authorization for Radiotherapy equipment and accessories

Radiotherapy equipment and accessories

EPR authorization is mandatory for

Radiotherapy equipment and accessories

Category : EPR Authorization

EEE Code : MDW1

Radiation therapy delivery and cancer treatment depend heavily on radiotherapy accessories and equipment. Indian Technical Standard MDW1 describes the manufacturing and quality requirements for these specialty medical equipment in India. It lays out precise technical requirements, quality standards, safety precautions, and testing protocols that producers of radiotherapy accessories and equipment must follow.

These specifications guarantee that these products are designed, produced, and evaluated in compliance with accepted quality standards. This entails making certain of their functionality, security, and adherence to Indian medical equipment regulations. Manufacturers who comply with these requirements support the country's efforts to improve patient safety, fight cancer, and enhance healthcare.

Note: Manufacturers of radiation equipment and related accessories are required to have an EPR Registration Certificate.

EPR Authorization highlights the manufacturers' obligations to make sure that their products are disposed of, recycled, and managed sustainably, especially when it comes to medical equipment like radiation devices. Regarding radiotherapy equipment and accessories, EPR authorization is important since it helps minimize electronic waste and encourage environmentally friendly practices in the medical field.


About Extended Producer Responsibility (EPR) Authorization for E-Waste

An essential program to handle the expanding problem of managing electronic trash, or "e-waste," is called EPRA, or Extended Producer's Responsibility Authorization. Securing EPR authorization from the State Pollution Control Boards (SPCBs) and receiving the EPR Registration Certificate from the Central Pollution Control Board (CPCB) are the two steps in the process of obtaining EPR authorization. With the help of EPRA, manufacturers and importers of electronic goods will take over management of e-waste from consumers and local governments. Electronics importers and manufacturers are obligated by EPRA to assume full responsibility for the whole lifecycle of their products, from manufacturing to disposal. Establishing and financing collection networks, recycling centers, and appropriate e-waste disposal techniques are all part of this. 


Required Documents for Extended Producer Responsibility (EPR) Authorization for E-Waste

  • Address Proof Documents
  • Product Information (including model numbers and production/import history)
  • Valid BIS License
  • CPCB Certification

For more detailed information, please click here.


Registration Process for Extended Producer Responsibility (EPR) Authorization for E-Waste

Step 1: Fill out the application form

Step 2: Attach all the required documents

For more detailed information, please click here


Why Choose Brand Liaison?

Brand Liaison offers valuable assistance in obtaining an EPR Registration Certificate for Radiotherapy equipment and accessories, Our services include:

  • Expert guidance
  • Streamline process
  • Comprehensive support
  • Cost-effective solutions
  • Time efficient

For a more in-depth understanding of the documentation and procedures involved in obtaining EPR Registration, feel free to connect with our team of experts at +91-9250056788 or +91-8130856678.



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